Kainate-binding, human CNS receptors of the EAA3 family

ABSTRACT

Neurotransmission by excitatory amino acids (EAAs) such as glutamate is mediated via membrane-bound surface receptors. DNA coding for one family of the kainate-binding type of EAA receptor, has now been isolated and the receptor protein characterized. Herein described are recombinant cell lines which produce the EAA receptor as a heterologous membrane-bound product. Also described are related aspects of the invention, which are of commercial significance. Included is use of the cell lines as a tool for discovery of compounds which modulate EAA receptor stimulation.

This application is a division, of application Ser. No. 07/989,793, filed Dec. 11, 1992, now abandoned.

FIELD OF THE INVENTION

This invention is concerned with applications of recombinant DNA technology in the field of neurobiology. More particularly, the invention relates to the cloning and expression of DNA coding for excitatory amino acid (EAA) receptors, especially human EAA receptors.

BACKGROUND OF THE INVENTION

In the mammalian central nervous system (CNS), the transmission of nerve impulses is controlled by the interaction between a neurotransmitter substance released by the “sending” neuron which then binds to a surface receptor on the “receiving” neuron, to cause excitation thereof. L-glutamate is the most neurotransmitter in the CNS, and mediates the major excitatory pathway is vertebrates. Glutamate is therefore referred to as an excitatory amino acid (EAA) and the receptors which respond to it are variously referred to as glutamate receptors, or more commonly as EAA receptors.

Using tissues isolated from mammalian brain, and various synthetic EAA receptor agonists, knowledge of EAA receptor pharmacology has been refined somewhat. Members of the EAA receptor family are now grouped into three main types based on differential binding to such agonists. One type of EAA receptor, which in addition to glutamate also binds the agonist NMDA (N-methyl-D-aspartate), is referred to as the NMDA type of EAA receptor. Two other glutamate-binding types of EAA receptor, which do not bind NMDA, are named according to their preference for binding with two other EAA receptors agonists, namely AMPA (α-amino-3-hydroxy-5-methyl-isoxazole-4-propionate), and kainate. Particularly, receptors which bind glutamate but not NMDA, and which bind with greater affinity to kainate than to AMPA, are referred to as kainate type EAA receptors. Similarly, those EAA receptors which bind glutamate but not NMDA, and which bind AMPA with greater affinity than kainate are referred to as AMPA type EAA receptors.

The glutamate-binding EAA receptor family is of great physiological and medical importance. Glutamate is involved in many aspects of long-term potentiation (learning and memory), in the development of synaptic plasticity, in epileptic seizures, in neuronal damage caused by ischemia following stroke or other hypoxic events, as well as in other forms of neurodegenerative processes. However, the development of therapeutics which modulate these processes has been very difficult, due to the lack of any homogeneous source of receptor material with which to discover selectively binding drug molecules, which interact specifically at the interface of the EAA receptor. The brain derived tissues currently used to screen candidate drugs are heterogeneous receptor sources, possessing on their surface many receptor types which interfere with studies of the EAA receptor/ligand interface of interest. The search for human therapeutics is further complicated by the limited availability of brain tissue of human origin. It would therefore be desirable to obtain cells that are genetically engineered to produce only the receptor of interest. With cell lines expressing cloned receptor genes, a substrate which is homogeneous for the desired receptor is provided, for drug screening programs.

Non-human cDNAs which appear to encode the kainate-type of receptor have been reported. Egebjerg et al. (Nature 351: 745, 1991) and WO91/06648, each describe the isolation of a cDNA from rat called GluR6 which, although related by sequence to AMPA receptor genes, forms a receptor which is not activated by AMPA but rather by glutamate, quisqualate, and preferentially, kainate. Other kainate binding proteins, which do not readily exhibit ion channel properties when expressed in a homomeric fashion, have also been cloned from frog (Wada et al., Nature 342: 684, 1989), chicken (Gregor et al., Nature 342: 689, 1989; Eshar et al., FEBS Lett. 297: 257, 1992), mouse (Sakimura et al., Neuron 8: 267, 1992) and rat (Werner et al., Nature 351: 742, 1991; Bettler et al., Neuron 8: 257, 1992; Herb et al., Neuron 8: 775, 1992).

There has emerged from these molecular cloning advances a better understanding of the structural features of EAA receptors and their subunits, as they exist in the rat brain. According to the current model of EAA receptor structure, each is heteromeric in structure, consisting of individual membrane-anchored subunits, each having four transmembrane regions, and extracellular domains that dictate ligand binding properties to some extent and contribute to the ion-gating function served by the receptor complex.

In the search for therapeutics useful to treat CNS disorders in humans, it is highly desirable to obtain knowledge of human EAA receptors. A specific understanding of human receptors would provide a means to screen for compounds that react therewith, i.e. to stimulate or inhibit receptor activity, and thus, provides a means to identify compounds having potential therapeutic utility in humans. Non-human mammalian models are not suitable for this purpose despite significant receptor sequence homology as minute sequence differences between species homologues of the same receptor from different species can cause dramatic pharmacological variation (Oksenberg et al., Nature, 360: 161, 1992). It is therefore particularly desirable to provide cloned cDNA encoding human EAA receptors, and cell lines expressing these receptors in a homogeneous fashion, in order to generate a proper screening method for compounds therapeutically useful in humans. These, accordingly, are objects of the present invention.

It is another object of the present invention to provide in isolated form a DNA molecule which codes for a human EAA receptor.

It is another object of the present invention to provide a cell that has been genetically engineered to produce a kainate-binding human EAA receptor.

Other objects of the present invention will be apparent from the following description of the invention.

SUMMARY OF THE INVENTION

Polynucleotides coding for a family of EAA receptors which in addition to binding glutamate with an affinity typical of EAA receptors, also exhibit ligand binding properties characteristic of kainate-type EAA receptors, have now been identified and characterized. A representative member of this human EAA receptor family is herein designated human EAA3a. Sequence-related polynucleotides coding for naturally occurring variants of the human EAA3a receptor have also been identified, and constitute additional members of this receptor family, herein referred to as the human EAA3 receptor family.

The present invention thus provides, in one of its aspects, an isolated polynucleotide, consisting either of DNA or of RNA, which codes for a human EAA3 receptor or for a kainate-binding fragment thereof.

In another aspect of the present invention, there is provided a cell that has been genetically engineered to produce a kainate-binding, human EAA receptor belonging to the herein-defined EAA3 family. In related aspects of the present invention, there are provided recombinant DNA constructs and relevant methods useful to create such cells.

In another aspect of the present invention, there is provided a method for evaluating interaction between a test ligand and a human EAA receptor, which comprises the steps of incubating the test ligand with a genetically engineered cell of the present invention, or with a membrane preparation derived therefrom, and then assessing said interaction by determining receptor/ligand binding.

Other aspects of the present invention, which encompass various applications of the discoveries herein described, will become apparent from the following detailed description, and from the accompanying drawings, in which:

BRIEF REFERENCE TO THE DRAWINGS

FIGS. 1A-1J provide the nucleotide sequence (SEQ ID NO:1) of a cDNA insert comprising DNA coding for an excitatory amino acid receptor of the present invention, and the deduced amino acid sequence (SEQ ID NO: 2) thereof;

FIG. 2 illustrates with plasmid maps the strategy used to construct a vector harbouring the full-length DNA sequence illustrated in FIGS. 1A-1J;

FIG. 3 (SEQ ID NO: 17 ) illustrates with plasmid maps the strategy used to construct expression vectors harbouring the DNA sequence illustrated in FIGS. 1A-1J;

FIGS. 4A-4C show, with reference to FIGS. 1A-1J, compare the DNA and amino acid sequences of naturally occurring variants to the DNA sequence of the EAA receptor illustrated in FIGS. 1A-1J (these sequences are also shown in SEQ ID NOS: 3-14); and

FIG. 5 illustrates the ligand-binding property of an EAA receptor expressed from the coding region provided in FIGS. 1A-1J.

DETAILED DESCRIPTION OF THE INVENTION AND ITS PREFERRED EMBODIMENTS

The invention relates to excitatory amino acid (EAA) receptors of human origin, and is directed more particularly to a novel family of kainate-type human EAA receptors, herein designated the human EAA3 receptor family. As used herein, the term “human EAA3 receptor” is intended to embrace the human EAA3a receptor, and kainate-binding variants of the EAA3a receptor that are structurally related thereto, i.e. share at least 97% amino acid identity including naturally occurring and synthetically derived variants of the EAA3a receptor. Naturally occurring variants of the human EAA3a receptor include particularly the receptors herein designated EAA3b, EAA3c and EAA3d. Synthetically derived variants of the human EAA3a receptor include kainate-binding variants that incorporate one or more, e.g. 1-56, amino acid deletions or additions relative to the EAA3a receptor, or one or more amino acid substitutions, e.g. 1-32 amino acid substitutions relative to the EAA3a receptor.

The term “kainate-binding”, as it is used herein with respect to EAA3 receptors, and variants and fragments thereof, is meant to encompass those receptors, variants and fragments that display greater binding affinity for kainate than for either glutamate, AMPA or NMDA, as determined in assays of conventional design, such as the assays herein described.

Each of the naturally occurring members of the EAA3 receptor family possesses structural features characteristic of EAA receptors in general, including extracellular amino (N-) and carboxy-terminal (C-terminal) regions, as well as four internal hydrophobic domains which serve to anchor the receptor within the cell surface membrane. The particular human EAA receptor designated EAA3a is a protein characterized structurally as a single polypeptide chain that is produced initially in precursor form bearing a 30 residue N-terminal signal peptide, and is transported to the cell surface in mature form i.e. lacking the signal peptide and consisting of 875 amino acids arranged in the sequence illustrated, by single letter code, in FIGS. 1A-1J (SEQ ID NO: 2). Unless otherwise stated, the term “EAA3 receptor” refers to the mature form of the receptor protein, and amino acid residues of EAA3 receptors are accordingly numbered with reference to the mature protein sequence. With respect to structural domains to the receptor, hydropathy analysis reveals four putative transmembrane domains, one spanning residues 533-552 inclusive (TM-1), another spanning residues 574-594 (TM-2), a third spanning residues 605-623 (TM-3) and the fourth spanning residues 790-810 (TM-4). Based on this assignment, it is likely that the human EAA3a receptor structure, in its natural membrane-bound form, consists of a 532 amino acid N-terminal extracellular domain, followed by a hydrophobic region containing the four transmembrane domains and an extracellular, 65 amino acid C-terminal domain.

As shown in FIGS. 4A-4C (and in SEQ ID NOS. 3-14), three structurally related variants of the EAA3a receptor, which occur naturally in human brain tissue, have also been identified and are herein designated the EAA3b, EAA3c and EAA3d receptors. As deduced from nucleotide sequences of the genes coding for them, the EAA3b variant shares greater than 99% amino acid identity with EAA3a, differing only by a single amino acid at position 639 which is an aspartate residue in the EAA3a receptor and an asparagine residue in the EAA3b receptor (FIG. 4A, SEQ ID NOS. 3-6). The EAA3c receptor, on the other hand, is a truncated version of EAA3a in which 40 amino acids have been eliminated from the C-terminus. Additionally, the last eleven amino acid residues at the C-terminus of EAA3c, i.e. amino acids at positions 826 to 836, differ from those in the corresponding region of EAA3a as shown in FIG. 4B (SEQ ID NOS :7-10). In comparison to EAA3a, the EAA3d receptor has a 56 amino acid deletion at its N-terminal end, i.e. the amino acids at positions 6 to 61 in EAA3a are deleted from EAA3d (FIG. 4C, SEQ ID NOS. 11-14).

Like other members of the human EAA3 receptor family, EAA3a is characterized by a pharmacological profile, i.e. a ligand binding “signature”, that points strongly to a kainate-type pharmacology, as distinct from other excitatory amino acid receptor types, such as NMDA and AMPA. In addition, and despite the understanding that kainate binding receptors require a multi- and perhaps heteromeric subunit structure to function in the pharmacological sense, it has been found that cells producing the unitary EAA3a receptor do, independently of association with other receptor subunits, provide a reliable indication of excitatory amino acid binding. Thus, in a key aspect of the present invention, the human EAA3a receptor is exploited for the purpose of screening candidate compounds for the ability to interact with the present receptors and/or the ability to compete with endogenous EAA receptor ligands and known synthetic analogues thereof, for EAA receptor interaction.

For use in assessing interaction between the receptor and a test ligand, it is desirable to construct by application of genetic engineering techniques a mammalian cell that produces a human EAA3 receptor in functional form as a heterologous product. The construction of such cell lines is achieved by introducing into a selected host cell a recombinant DNA construct in which DNA coding for a secretable form of the human EAA3 receptor, i.e., a form bearing either its native signal peptide or a functional, heterologous equivalent thereof, is associated with expression controlling elements that are functional in the selected host to drive expression of the receptor-encoding DNA, and thus elaborate the desired EAA3 receptor protein. Such cells are herein characterized as having the receptor-encoding DNA incorporated “expressibly” therein. The receptor-encoding DNA is referred to as “heterologous” with respect to the particular cellular host if such DNA is not naturally found in the particular host.

It is most desirable to use a mammalian cell host to produce EAA3 receptors due to the mammalian origin of the present human EAA3 receptors; however, other suitably engineered eukaryotic and prokaryotic hosts may also be employed to produce EAA3 receptors. Accordingly, bacterial hosts such as E. coli and B. subtilis, fungal hosts such as Aspergillus and yeast and insert cell hosts such as Spodoptera frugiperda, are examples of non-mammalian hosts that may also be used to produce EAA3 receptors of the present invention.

The particular cell type selected to serve as host for production of the human EAA3 receptor can be any of several cell types currently available in the art, but should not of course be a cell type that in its natural state elaborates a surface receptor that can bind excitatory amino acids, and so confuse the assay results sought from the engineered cell line. Generally, such problems are avoided by selecting as host a non-neuronal cell type, and can further be avoided using non-human cell lines, as is conventional. It will be appreciated that neuronal- and human-type cells may nevertheless serve as expression hosts, provided that “background” binding to the test ligand is accounted for in the assay results.

According to one embodiment of the present invention, the cell line selected to serve as host for EAA3 receptor production is a mammalian cell. Several types of such cell lines are currently available for genetic engineering work, and these include the chinese hamster ovary (CHO) cells for example of K1 lineage (ATCC CCL 61) including the Pro5 variant (ATCC CRL 1281); the fibroblast-like cells derived from SV40-transformed African Green monkey kidney of the CV-1 lineage (ATCC CCL 70), of the COS-1 lineage (ATCC CRL 1650) and of the COS-7 lineage (ATCC CRL 1651); murine L-cells, murine 3T3 cells (ATCC CRL 1658), murine C127 cells; human embryonic kidney cells of the 293 lineage (ATCC CRL 1573), human carcinoma cells including those of the HeLa lineage (ATCC CCL 2), and neuroblastoma cells of the lines IMR-32 (ATCC CCL 127), SK-N-MC (ATCC HTB 10) and SK-N-SH (ATCC HTB 11).

A variety of gene expression systems have been adapted for use with these hosts and are now commercially available, and any one of these systems can be exploited to drive expression of the EAA3 receptor-encoding DNA. These systems, available typically in the form of plasmidic vectors, incorporate expression cassettes the functional components of which include DNA constituting expression controlling sequences, which are host-recognized and enable expression of the receptor-encoding DNA when linked 5′ thereof. The systems further incorporate DNA sequences which terminate expression when linked 3′ of the receptor-encoding region. Thus, for expression in the selected mammalian cell host, there is generated a recombinant DNA expression construct in which DNA coding for a secretable form of the receptor is linked with expression controlling DNA sequences recognized by the host, and which include a region 5′ of the receptor-encoding DNA to drive expression, and a 3′ region to terminate expression. The plasmidic vector harbouring the expression construct typically incorporates such other functional components as an origin replication, usually virally-derived, to permit replication of the plasmid in the expression host and desirably also for plasmid amplification in a bacterial host, such as E. coli. To provide a marker enabling selection of stably transformed recombinant cells, the vector will also incorporates a gene conferring some survival advantage of the transformants, such as a gene coding for neomycin resistance in which case the transformants are plated in medium supplemented with neomycin.

Included among the various recombinant DNA expression systems that can be used to achieve mammalian cell expression of the receptor-encoding DNA are those that exploit promoters of viruses that infect mammalian cells, such as the promoter from the cytomegalovirus (CMV), the Rous sarcoma virus (RSV), simian virus (SV40), murine mammary tumor virus (MMTV) and others. Also useful to drive expression are promoters such as the LTR of retroviruses, insect cell promoters such as those regulated by temperature, and isolated from Drosophila, as well as mammalian gene promoters such as steroid-inducible promoters and those regulated by heavy metals i.e., the metallothionein gene promoter.

For incorporation into the recombinant DNA expression vector, DNA coding for the desired EAA3 receptor, e.g. the EAA3a receptor or a kainate-binding variant thereof, can be obtained by applying selected techniques of gene isolation or gene synthesis. As described in more detail in the examples herein, the EAA3a receptor, and the EAA3b, EAA3c, and EAA3d variants thereof, are encoded within the genome of human brain tissue, and can therefore be obtained by careful application of conventional gene isolation and cloning techniques. This typically will entail extraction of total messenger RNA from a fresh source of human brain tissue, such as cerebellum or hippocampus tissue and preferably fetal brain tissue, followed by conversion of message to cDNA and formation of a library in for example a bacterial plasmid, more typically a bacteriophage. Such bacteriophage harbouring fragments of the human DNA are typically grown by plating on a lawn of susceptible E. coli bacteria, such that individual phase plaques or colonies can be isolated. The DNA carried by the phage colony is then typically immobilized on a nitrocellulose or nylon-based hybridization membrane, and then hybridized, under carefully controlled conditions, to a radioactively (or otherwise) labelled oligonucleotide probe of appropriate sequence to identify the particular phage colony carrying receptor-encoding DNA or fragment thereof. Typically, the gene or a portion thereof so identified is subcloned into a plasmidic vector for nucleic acid sequence analysis.

Having herein provided the nucleotide sequence of various human EAA3 receptors, it will be appreciated that automated techniques of gene synthesis and/or amplification can be performed to generate DNA coding therefor. Because of the length of EAA3 receptor-encoding DNA, application of automated synthesis may require stage gene construction, in which regions of the gene up to about 300 nucleotides in length are synthesized individually and then ligated in correct succession for final assembly. Individually synthesized gene regions can be amplified prior to assembly, using polymerase chain reaction (PCR) technology.

The application of automated gene synthesis techniques provides an opportunity for generating sequence variants of naturally occurring members of the EAA3 gene family. It will be appreciated that polynucleotides coding for the EAA3 receptors herein described can be generated by substituting synonymons codons for those represented in the naturally occurring polynucleotide sequences herein identified. In addition, polynucleotides coding for synthetic variants of the EAA3 receptors herein described can be generated which for example incorporate one or more single amino acid substitutions, deletions or additions. Since it will for the most part be desirable to retain the natural ligand binding profile of the receptor for screening purposes, it is desirable to limit amino acid substitutions, for example to the so-called conservative replacements in which amino acids of like charge are substituted, and to limit substitutions to those sites less critical for receptor activity e.g. within about the first 20 N-terminal residues of the mature receptor, and such other regions as are elucidated upon receptor domain mapping.

With appropriate template DNA in hand, the technique of PCR amplification may also be used to directly generate all or part of the final gene. In this case, primers are synthesized which will prime the PCR amplification of the final product, either in one piece, or in several pieces that may be ligated together. This may be via step-wise ligation of blunt ended, amplified DNA fragments, or preferentially via step-wise ligation of fragments containing naturally occurring restriction endonuclease sites. In this application, it is possible to use either cDNA or genomic DNA as the template for the PCR amplification. In the former case, the cDNA template can be obtained from commercially available or self-constructed cDNA libraries of various human brain tissues, including hippocampus and cerebellum.

Once obtained, the receptor-encoding DNA is incorporated for expression into any suitable expression vector, and host cells are transfected therewith using conventional procedures, such as DNA-mediated transformation, electroporation, microinjection, or particle gun transformation. Expression vectors may be selected to provide transformed cell lines that express the receptor-encoding DNA either transiently or in a stable manner. For transient expression, host cells are typically transformed with an expression vector harbouring an origin of replication functional in a mammalian cell. For stable expression, such replication origins are unnecessary, but the vectors will typically harbour a gene coding for a product that confers on the transformants a survival advantage, to enable their selection. Genes coding for such selectable markers include the E. coli gpt gene which confers resistance to mycophenolic acid, the neo gene from transposon Tn5 which confers resistance to the antibiotic G418 and to neomycin, the dhfr sequence from murine cells or E. coli which changes the phenotype of DHFR− cells into the DHFR+ cells, and the tk gene of herpes simplex virus, which makes TK− cells phenotypically TK+ cells. Both transient expression and stable expression can provide transformed cell lines, and membrane preparations derived therefrom, for use in ligand screening assays.

For use in screening assays, cells transiently expressing the receptor-encoding DNA can be stored frozen for later use, but because the rapid rate of plasmid replication will lead ultimately to cell death, usually in a few days, the transformed cells should be used as soon as possible. Such assays may be performed either with intact cells, or with membrane preparations derived from such cells. The membrane preparations typically provide a more convenient substrate for the ligand binding experiments, and are therefore preferred as binding substrates. To prepare membrane preparations for screening purposes, i.e., ligand binding experiments, frozen intact cells are homogenized while in cold water suspension and a membrane pellet is collected after centrifugation. The pellet is then washed in cold water, and dialyzed to remove endogenous EAA ligands such as glutamate, that would otherwise compete for binding in the assays. The dialyzed membranes may then be used as such, or after storage is lyophilized form, in the ligand binding assays. Alternatively, intact, fresh cells harvested about two days after transient transfection or after about the same period following fresh plating of stably transfected cells, can be used for ligand binding assays by the same methods as used for membrane preparations. When cells are used, the cells must be harvested by more gentle centrifugation so as not to damage them, and all washing must be done in a buffered medium, for example in phosphate-buffered saline, to avoid osmotic shock and rupture of the cells.

The EAA3 receptors of the present invention are per se functional in an electrophysiological context, and are therefore useful, in the established manner, in screening test ligands for their ability to modulate ion channel activity. The present invention thus further provides, as a ligand screening technique, a method of detecting interaction between a test ligand and a human CNS receptor, which comprises the steps of incubating the test ligand with a human EAA3 receptor-producing cell or with a membrane preparation derived therefrom, and then measuring ligand-induced electrical current across said cell or membrane.

As an alternative to using cells that express receptor-encoding DNA, ligand characterization may also be performed using cells, for example Xenopus oocytes, that yield functional membrane-bound receptor following introduction of messenger RNA coding for the EAA3 receptor. In this case, the EAA3 receptor gene of the invention is typically subcloned into a plasmidic vector such that the introduced gene may be easily transcribed into RNA via an adjacent RNA transcription promoter supplied by the plasmidic vector, for example the T3 or T7 bacteriophage promoters. RNA is then transcribed from the inserted gene in vitro, and can then be injected into Xenopus oocytes. Following the injection of nL volumes of an RNA solution, the oocytes are left to incubate for up to several days, and are then tested in either intact form or as a membrane preparation for the ability to bind a particular ligand molecule supplied in a bathing solution. Since functional EAA receptors act in part by operating a membrane channel through which ions may selectively pass, the functioning of the receptor in response to a particular ligand molecule in the bathing solution may typically be measured as an electrical current utilizing microelectrodes inserted into the cell or placed on either side of a cell-derived membrane preparation using the “patch-clamp” technique.

The binding of a candidate ligand to a selected human EAA3 receptor of the invention is evaluated typically using a predetermined amount of cell-derived membrane (measured for example by protein determination), generally from about 25 ug to 100 ug. Generally, competitive binding assays will be useful to evaluate the affinity of a test compound relative to kainate. This competitive binding assay can be performed by incubating the membrane preparation with radiolabelled kainate, for example [3H]-kainate, in the presence of unlabelled test compound added at varying concentrations. Following incubation, either displaced or bound radiolabelled kainate can be recovered and measured, to determine the relative binding affinities of the test compound and kainate for the particular receptor used as substrate. In this way, the affinities of various compounds for the kainate-type human EAA receptors can be measured.

In addition to using the receptor-encoding DNA to construct cell lines useful for ligand screening, expression of the DNA can, according to another aspect of the invention, be performed to produce fragments of the receptor in soluble form, for structure investigation, to raise antibodies and for other experimental uses. It is expected that kainate-binding fragments, i.e., the portion of the EAA3 receptor responsible for binding a ligand molecule, resides on the outside of the cell, i.e., is extracellular. It is therefore desirable in the first instance to facilitate the characterization of the receptor-ligand interaction by providing such kainate binding fragments in quantity and in isolated form, i.e., free from the remainder of the receptor. To accomplish this, the full-length EAA3 receptor-encoding DNA may be modified by site-directed mutagenesis, to introduce a translational stop codon into the extracellular N-terminal region, immediately 5′ of the first transmembrane domain (TM1), i.e., before the residue 533 codon as shown in FIGS. 1A-1J (SEQ ID NO:1). Since there will no longer be produced any transmembrane domain(s) to “anchor” the receptor into the membrane, expression of the modified gene will result in the secretion, in soluble form, of only the extracellular ligand-binding domain. Standard ligand-binding assays may then be performed to ascertain the degree of binding of a candidate compound to the extracellular domain so produced. It may of course be necessary, using site-directed mutagenesis, to produce different versions of the extracellular regions, in order to map the ligand binding domain with precision. It will also be appreciated that the length of the fragment may be varied, i.e. to lengths less than the entire 533 amino acid extracellular N-terminal domain.

Alternatively, it may be desirable to produce an extracellular domain of the receptor which is not derived from the N-terminus of the mature protein, but rather from the C-terminus, for example domains immediately following the fourth transmembrane domain (TM4), i.e., residing between amino acid residues 811 and 875 inclusive as shown in FIGS. 1A-1J (SEQ ID NO:1). In this case, site-directed mutagenesis and/or PCR-based amplification techniques may readily be used to provide a defined fragment of the gene encoding the receptor domain of interest. Direct peptide synthesis may also be used to make the desired C-terminal fragment, or as noted above, desired N-terminal fragments. Such a DNA sequence may be used to direct the expression of the desired receptor fragment, either intracellularly, or in secreted fashion, provided that the DNA encoding the gene fragment is inserted adjacent to a translation start codon provided by the expression vector, and that the required translation reading frame is carefully conserved.

It will be appreciated that the production of such extracellular ligand binding domains may be accomplished in a variety of host cells. Mammalian cells such as CHO cells may be used for this purpose, the expression typically being driven by an expression promoter capable of high-level expression, for example the CMV (cytomegalovirus) promoter. Alternately, non-mammalian cells, such as insect Sf9 (Spodoptera frugiperda) cells may be used, with the expression typically being driven by expression promoters of the baculovirus, for example the strong, late polyhedrin protein promoter. Filamentous fungal expression systems may also be used to secrete large quantities of such extracellular domains of the EAA receptor. Aspergillus nidulans, for example, with the expression being driven by the a1cA promoter, would constitute such an acceptable system. In addition to such expression hosts, it will be further appreciated that any prokaryotic or other eukaryotic expression system capable of expressing heterologous genes or gene fragments, whether intracellularly or extracellularly would be similarly acceptable.

For use particularly in detecting the presence and/or location of an EAA3 receptor, for example in brain tissue, the present invention also provides, in another of its aspects, labelled antibody to a human EAA3 receptor. To raise such antibodies, there may be used as immunogen either the intact, soluble receptor or an immunogenic fragment thereof, produced in a microbial or mammalian cell host as described above or by standard peptide synthesis techniques. Regions of the EAA3a receptor particularly suitable for use as immunogenic fragments include those corresponding in sequence to an extracellular region of the receptor, or a portion of the extracellular region, such as peptides consisting of residues 1-532 or fragments thereof, including particularly residues 186-201 or 485-528, and peptides corresponding to the region between transmembrane domains TM-2 and TM-3, such as a peptide consisting of residues 595-604. Peptides consisting of the C-terminal domain (residues 811-875), or fragments thereof may also be used for the raising of antibodies. Substantially the same region of the human EAA3b, EAA3c and EAA3d receptor may also be used for production of antibodies against this receptor.

The raising of antibodies to the desired EAA3 receptor or immunogenic fragment can be achieved, for polyclonal antibody production, using immunization protocols of conventional design, and any of a variety of mammalian hosts, such as sheep, goats and rabbits. Alternatively, for monoclonal antibody production, immunocytes such as splenocytes can be recovered from the immunized animal and fused, using hybridoma technology, to myeloma cells. The fusion products, i.e. hybridomas, are then screened by culturing in a selection medium, and cells producing antibody are recovered for continuous growth, and antibody recovery. Recovered antibody can then be coupled covalently to a reporter molecule, i.e. a detectable label such as a radiolabel, enzyme label, luminescent label or the like, using linker technology established for this purpose, to form a specific probe for EAA3 receptors.

In detectably labelled form, e.g. radiolabelled form, DNA or RNA coding for the human EAA3 receptor, and selected regions thereof, may also be used, in accordance with another aspect of the present invention, as hybridization probes for example to identify sequence-related genes resident in the human or other mammalian genomes (cDNA libraries) or to locate the EAA3-encoding DNA in a specimen, such as brain tissue. This can be done using either the intact coding region, or a fragment thereof having radiolabelled e.g. ³²P, nucleotides incorporated therein. To identify the EAA3-encoding DNA in a specimen, it is desirable to use either the full length cDNA coding therefor, or a fragment which is unique thereto. With reference to FIG. 1 (SEQ ID NO: 1) and the nucleotide numbering appearing thereon, such nucleotide fragments include those comprising at least about 17 nucleic acids, and otherwise corresponding in sequence to a region coding for the N-terminus or C-terminus of the receptor, or representing a 5′-untranslated or 3′-untranslated region thereof. Examples of suitable nucleotide fragments for this purpose include nucleotides 426-446 and nucleotides 1251-1271 of EAA3a. These sequences, among others, as well as the intact gene itself, may also be used of course to clone EAA3-related human genes, particularly cDNA equivalents thereof, by standard hybridization techniques.

Embodiments of the present invention are described in detail in the following non-limiting Examples.

EXAMPLE 1 Isolation of DNA Coding for the Human EAA3a Receptor

cDNA coding for the human EAA3a receptor was identified by probing human fetal brain cDNA that was obtained as an EcoRI-based lambda phage library (lambda ZAP) from Stratagene Cloning Systems (La Jolla, Calif., U.S.A.). The cDNA library was screened using an oligonucleotide probe having the following specific sequence (SEQ ID NO: 15):

5′-ATCGGCGGCATCTTCATTGTTCTGGCTGCAGGACTCGTGC-3′

The fetal brain cDNA library was screened under the following hybridization conditions; 6xSSC, 25% formamide, 5× Denhardt's solution, 10 mM Na₂HPO₄ buffer, 0.5% sodium pyrophosphate, 0.5% SDS, 100 μg/ml denatured salmon sperm DNA. 42° C. Filters were washed with 6xSSC containing 0.5% SDS at 25° C. for 5 minutes, followed by a 15 minute wash at 42° C. with 2xSSC containing 0.5% SDS. The final wash was with 1xSSC containing 0.5% SDS at 50° C. for 15 minutes. Filters were exposed to X-ray film (Kodak) overnight. Of 10⁶ clones screened, only two cDNA inserts were identified; one of about 0.9 kb designated RKCSFG72, and another of about 2.7 kb designated RKCS5F81. For sequencing, the '72 and '81 phages were plaque purified, then excised as phagemids according to the supplier's specifications, to generate insert-carrying Bluescript-SK variants of the phagemid vectors. Sequencing of the '72 clone across its entire sequence revealed an open reading frame representing the C-terminal region but no putative termination codon. Sequencing across the '81 insert revealed a DNA sequence with about 80% identity with the '72 clone. The '81 clone displayed significant overlap to the '72 clone and included an additional 5′ sequence.

Since no initiation and termination codons were apparent in the '72 sequence, the 5′ and 3′ regions of the '72 clone was sought. For this purpose, a 2.0 kb EcoRI fragment representing the '81 clone and a 0.9 kb EcoRI fragment representing the '72 clone was isolated. ³²P-labelled, and then used to re-screen the same fetal brain cDNA library under the following hybridization conditions: 6xSSC, 25% formamide, 5× Denhardt's solution, 0.5% SDS, 100 μg/ml denatured salmon sperm DNA, 30° C. Filters were washed twice with 2xSSC containing 0.5% SDS at 25° C. for 5 minutes, followed by a 15 minute final wash at 42° C. with 2xSSC containing 0.5% SDS. Filters were exposed to X-ray film (Kodak) overnight. Of 10⁶ clones screened, only two cDNA were identified, one of about 1.5 kb designated RKCS221, and the another of about 1.8 kb designated RKC41. Sequencing the entire '221 inserted revealed more of the 5′ sequence of the '72 clone as well as a termination codon and about 250 bases of the 3′ non-coding region. Sequencing the entire '41 insert revealed more of the 5′ sequence but still did not reveal an initiation codon.

Thus, the same fetal brain cDNA library was screened using an oligonucleotide probe (based on the '41 sequence) capable of annealing to the 5′ region of the '41 sequence. The specific sequence (SEQ ID NO:16) of the 32P-labelled probe is provided below:

5′-CCATCATTGAGAAGTGGTCC-3′

This probe was ³²P-labelled and then used to re-screen the same fetal brain cDNA library under the following hybridization conditions: 6xSSC, 50% formamide, 5× Denhardt's solution, 0.5% SDS, 100 μg/ml denatured salmon sperm DNA, 30° C. Filters were washed twice with 2xSSC containing 0.5% SDS at 25° C. for 5 minutes, followed by a 15 minute final wash at 42° C. with 2xSSC containing 0.5% SDS. Filters were exposed to X-ray film (Kodak) overnight. Of 10⁶ clones screened, a single cDNA insert was identified of about 1.7 kb designated RKS71. The '71 insert, when sequenced, revealed the initiation codon together with about 417 bases of 5′ non-coding region and a significant overlap with the '41 insert.

To provide the entire coding region of the receptor, the strategy depicted in FIG. 2 was then applied to generate the 6.3 kb phagemid pBS/humEAA3a which carries the intact EAA3a receptor-encoding DNA as a 3.3 kb NotI/HindIII insert in a 3.0 kb pBluescript phagemid background pBS/PF/RK571 is cut with NarI and Eco RV and pBS/7ES/RKC41 is cut with NarI and SmaI to produce a 1.4 Kbp segment. The resulting products are ligated. The ligated product is then cut with Kpn I, and PBS/5RP/RKC221 also is cut with Kpn I to produce a 1.2 Kbp segment. The two are ligated to produce pBS/humEAA3a. In FIG. 2, Sc represents Sac I, Sm represents Sma I, RI represents Eco RI, Nar represents Nar I, RV represents Eco RV, Kp represents Kpn I and N represent Not I. Phagemid pBS/humEAA3a was deposited under the terms of the Budapest Treaty with the American Type Culture Collection in Rockville, Md. USA on Nov. 12, 1992, and has been assigned accession number ATCC 75350.

EXAMPLE 2 Construction of Genetically Engineered Cells Producing the Human EAA3a Receptor

For transient expression in mammalian cells, cDNA encoding the EAA3a receptor was incorporated into the mammalian expression vector pcDNAI/Amp (pcDNAIA), which is available commercially from Invitrogen Corporation (San Diego, Calif., USA: catalogue number V490-20), as depicted in FIG. 3. In FIG. 2, Sc represents SacI, H3 represents Hind III, Sm represents Sma I, RI represents Eco RI, Nar represents Nar I, RV represents Eco RV, Kp represents Kpn I, N represent Not I and Xb represents Xba I. pcDNAIA is a multifunctional 4.8 kb plasmid vector designed for cDNA expression in eukaryotic systems, and cDNA analysis in prokaryotes. Incorporated on the vector are the CMV promoter and enhancer, splice segment and polyadenylation signal, an SV40 and Polyoma virus origin of replication, M13 origin to rescue single strand DNA for sequencing and mutagenesis, Sp6 and T7 RNA promoters for the production of sense and anti-sense RNA transcripts and a Col E1-like high copy plasmid origin. A polylinker is located appropriately downstream of the CMV promoter and 3′ of the T7 promoter.

pBS/humEAA3a is cut with Eco RV and Hind III, and 5′-d[AGCTTGCCGCCGC]-3′ and 3′-[ACGCCGGCG]]p-5′ with a Hind III/Not I adaptor at the 3′ end is then ligated. Briefly, the EAA3a-encoding cDNA insert was released from pBS/humEAA3a upon cutting with Not I as a 3.3 kb NotI/NotI fragment subsequent to insertion of a HindIII/NotI adaptor at the 3′ end of the insert. Following cutting with NotI and dephosphorylation of pcDNAIA, the 3.3 kb fragment was then incorporated at the NotI site in the pcDNAIA vector to form the expression vector pcDNAIA/humEAA3a.

For transient expression of the EAA3a-encoding DNA, monkey-derived, fibroblast-like cells of the COS-1 lineage (available from the American Type Culture Collection, Rockville, Md. as ATCC CRL 1650) were transfected with approximately 8 ng DNA (as pcDNAIA/humEAA3a) per 10⁶ COS cells, by DEAE-mediated DNA transfection and treated with chloroquine according to conventional procedures. Briefly, COS-1 cells were plated at a density of 5×10⁶ cells/dish and then grown for 24 hours in FBS-supplemented DMEM/F12 medium. Medium was then removed and cells were washed with PBS and then with medium. There was then applied on the cells 10 ml of a transfection solution containing DEAE dextran (0.4 mg/ml), 100 μM chloroquine, 10% NuSerum, DNA (0.4 mg/ml) in DMEM/F12 medium. After incubation for 3 hours at 37° C., cells were washed in PBS and medium as just described and then shocked for 1 minute with 10% DMSO in DMEM/F12 medium. Cells were allowed to grow for 2-3 days in 10% FBS-supplemented medium, and at the end of incubation dishes were placed on ice, the cells were washed with ice cold PBS and then removed by scraping. Cells were then harvested by centrifugation at 1000 rpm for 10 minutes and the cellular pellet was frozen in liquid nitrogen, for subsequent use in ligand binding assays. Northern blot analysis of a thawed aliquot of frozen cells confirmed expression of receptor-encoding cDNA in cells under storage.

In a like manner, stably transfected cell lines can also be prepared using two different cell types as host; CHO K1 and CHO Pro5. To construct these cell lines, cDNA coding for human EAA3a is incorporated into the mammalian expression vector pRC/CMV (Invitrogen), which enables stable expression. Insertion at this site places the cDNA under the expression control of the cytomegalovirus promoter and upstream of the polyadenylation site and terminator of the bovine growth hormone gene, and into a vector background comprising the neomycin resistance gene (driven by the SV40 early promoter) as selectable marker.

To introduce plasmids constructed as described above, the host CHO cells are first seeded at a density of 5×10⁵ in 10% FBS-supplemented αMEM medium. After growth for 24 hours, fresh medium is added to the plates and three hours later, the cells are transfected using the conventional calcium phosphate-DNA co-precipitation procedure. Briefly, 3 μg of DNA is mixed and incubated with buffered calcium solution for 10 minutes at room temperature. An equal volume of buffered phosphate solution is added and the suspension is incubated for 15 minutes at room temperature. Next, the incubated suspension is applied to the cells for 4 hours, removed and cells were shocked with medium containing 15% glycerol. Three minutes later, cells are washed with medium and incubated for 24 hours at normal growth conditions. Cells resistant to neomycin are selected in 10% FBS-supplemented alpha-MEM medium containing G418 (1 mg/ml). Individual colonies of G418-resistant cells are isolated about 2-3 weeks later, clonally selected and then propogated for assayed purposes.

EXAMPLE 3 Ligand Binding Assays

Transfected cells in the frozen state were resuspended in ice-cold distilled water using a hand homogenizer and centrifuged for 20 minutes at 50,000 g. The supernatant was discarded and the membrane pellet stored frozen at −70° C.

COS cell membrane pellets were suspended in ice cold 50 mM Tris-HCl (pH 7.55, 5° C.) and centrifuged again at 50,000 g for 10 minutes in order to remove endogenous glutamate that would compete for binding. Pellets were resuspended in ice cold 50 mM Tris-HCl (pH 7.55) buffer and the resultant membrane preparation was used as tissue source for binding experiments described below. Proteins were determined using the Pierce Reagent with BSA as standard.

Binding assays were then performed, using an amount of COS-derived membrane equivalent to 25-100 ug as judged by protein determination and selected radiolabelled ligand. In particular, for kainate binding assays, incubation mixtures consisted of 25-100 μg tissue protein and [vinylidene-3H] kainic acid (58 Ci/mmole, 80 nM final) in the cold incubation buffer, 1 ml final volume. Non-specific binding was in the presence of 1 mM L-glutamate. Samples were incubated on ice for 60 minutes, and bound and free ligand were then separated by rapid filtration using a PHD cell harvester and GF/B filters pre-soaked in ice-cold 0.3% polyethyleneimine. Filters were washed twice in 4 ml of the cold incubation buffer, then placed in scintillation vials with 5 ml of Beckman Ready-Protein Plus scintillation cocktail for counting.

For AMPA-binding assays, incubation mixtures consisted of 25-100 ug tissue protein and D,L-α-[5-methyl-3H]amino-3-hydroxy-5-methylisoxazole-4-propionic acid (3H-AMPA, 27.6 Ci/mmole, 10 nM final) with 0.1M KSCN and 2.5 mM CaCl₂ in the 1 ml final volume. Non-specific binding was determined in the presence of 1 mM L-glutamate. Samples were incubated on ice for 60 minutes in plastic minivials, and bound and free ligand were separated by centrifugation for 30 minutes at 50,000 g. Pellets were washed twice in 4 ml of the cold incubation buffer, then 5 ml of Beckman Ready-Protein Plus scintillation cocktail was added, for counting.

Assays performed in this manner, using membrane preparations derived from the EAA3a-producing COS cells, revealed specific [3H]-kainate binding of 167 fmol/mg protein at 80 nM, labelled ligand (FIGS. 4A-4C). Mock transfected cells exhibited no specific binding of any of the ligands tested. These results demonstrate clearly that the human EAA3a receptor is binding kainate specifically. This activity, coupled with the fact that there is little or no demonstrable binding of either AMPA or NMDA clearly assigns the EAA3a receptor to be of the kainate type of EAA receptor. Furthermore, this binding profile indicates that the receptor is functioning in an authentic manner, and can therefore reliably predict the ligand binding “signature” of its non-recombinant counterpart from the intact human brain. These features make the recombinant receptor especially useful for selecting and characterizing ligand compounds which bind to the receptor, and/or for selecting and characterizing compounds which may act by displacing other ligands from the receptor. The isolation of the EAA3a receptor gene in a pure form, capable of being expressed as a single, homogenous receptor species, therefore frees the ligand binding assay from the lack of precision introduced when complex, heterogeneous receptor preparations from human and non-human brains are sued to attempt such characterizations.

19 3385 base pairs nucleic acid double linear cDNA CDS 418..3132 mat_peptide 508..3132 sig_peptide 418..507 1 GAATTCCGTC TTCTTTCCCC CTTTTCCCTC CTCTGTCTGT GCCTATCCCC CGACTTTTGC 60 ATCTGACCAA AGGACGAATG AGGGAGACGT TCCTGCAGAT CGGGGCAGCA ACTTTCCTCA 120 GCTGGTCTCT GGGCTCCGGA GCCAGAGAGC GCTGATCCTC CGCGTCTGCG GCCCATGAAG 180 AGAGAGAGAG CCGTGATGGG CTAGCGACAG CACTGAGGAG CCCCGAGAGA GCTCAGCCTT 240 GCCAGCCAGC TCCGCGGTCC CACGCGGGTT CCCTCGAGCT CGCTCCGTGG GGAGCGCGCA 300 GCGTGCTTGG AACCGGAGCA TCCAGAGAGG ATGAGGCGGG GACCCGGCCC AAGTTGGGTG 360 CATCTCTCGG GCGTCCGGCA GCGGCTGTAT CTCGGCATGA ATTAAGAAGC TAGGAAG 417 ATG GAG CAC GGC ACA CTC CTC GCC CAG CCC GGG CTC TGG ACC AGG GAC 465 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp -30 -25 -20 -15 ACC AGC TGG GCA CTC CTC TAT TTC CTC TGC TAT ATC CTC CCT CAG ACC 513 Thr Ser Trp Ala Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr -10 -5 1 GCC CCG CAA GTA CTC AGG ATC GGA GGG ATT TTT GAA ACA GTG GAA AAT 561 Ala Pro Gln Val Leu Arg Ile Gly Gly Ile Phe Glu Thr Val Glu Asn 5 10 15 GAG CCT GTT AAT GTT GAA GAA TTA GCT TTC AAG TTT GCA GTC ACC AGC 609 Glu Pro Val Asn Val Glu Glu Leu Ala Phe Lys Phe Ala Val Thr Ser 20 25 30 ATT AAC AGA AAC CGA ACC CTG ATG CCT AAC ACC ACA TTA ACC TAT GAC 657 Ile Asn Arg Asn Arg Thr Leu Met Pro Asn Thr Thr Leu Thr Tyr Asp 35 40 45 50 ATC CAG AGA ATT AAC CTT TTT GAT AGT TTT GAA GCC TCG CGG AGA GCA 705 Ile Gln Arg Ile Asn Leu Phe Asp Ser Phe Glu Ala Ser Arg Arg Ala 55 60 65 TGT GAC CAG CTG GCT CTT GGT GTG GCT GCT CTC TTT GGC CCT TCC CAT 753 Cys Asp Gln Leu Ala Leu Gly Val Ala Ala Leu Phe Gly Pro Ser His 70 75 80 AGC TCC TCC GTC AGT GCT GTG CAG TCT ATT TGC AAT GCT CTC GAA GTT 801 Ser Ser Ser Val Ser Ala Val Gln Ser Ile Cys Asn Ala Leu Glu Val 85 90 95 CCA CAC ATA CAG ACC CGC TGG AAA CAC CCC TCG GTG GAC AAC AAA GAT 849 Pro His Ile Gln Thr Arg Trp Lys His Pro Ser Val Asp Asn Lys Asp 100 105 110 TTG TTT TAC ATC AAC CTT TAC CCA GAT TAT GCA GCT ATC AGC AGG GCG 897 Leu Phe Tyr Ile Asn Leu Tyr Pro Asp Tyr Ala Ala Ile Ser Arg Ala 115 120 125 130 ATC CTG GAT CTG GTC CTC TAT TAC AAC TGG AAA ACA GTG ACA GTG GTG 945 Ile Leu Asp Leu Val Leu Tyr Tyr Asn Trp Lys Thr Val Thr Val Val 135 140 145 TAT GAA GAC AGC ACA GGT CTA ATT CGT CTA CAA GAG CTC ATC AAA GCT 993 Tyr Glu Asp Ser Thr Gly Leu Ile Arg Leu Gln Glu Leu Ile Lys Ala 150 155 160 CCC TCC AGA TAT AAT ATT AAA ATC AAA ATC CGC CAG CTG CCC TCT GGG 1041 Pro Ser Arg Tyr Asn Ile Lys Ile Lys Ile Arg Gln Leu Pro Ser Gly 165 170 175 AAT AAA GAT GCC AAG CCT TTA CTC AAG GAG ATG AAG AAA GGC AAG GAG 1089 Asn Lys Asp Ala Lys Pro Leu Leu Lys Glu Met Lys Lys Gly Lys Glu 180 185 190 TTC TAT GTG ATA TTT GAT TGT TCA CAT GAA ACA GCC GCT GAA ATC CTT 1137 Phe Tyr Val Ile Phe Asp Cys Ser His Glu Thr Ala Ala Glu Ile Leu 195 200 205 210 AAG CAG ATT CTG TTC ATG GGC ATG ATG ACC GAA TAC TAT CAC TAC TTT 1185 Lys Gln Ile Leu Phe Met Gly Met Met Thr Glu Tyr Tyr His Tyr Phe 215 220 225 TTC ACA ACC CTG GAC TTA TTT GCT TTG GAT CTG GAA CTC TAT AGG TAC 1233 Phe Thr Thr Leu Asp Leu Phe Ala Leu Asp Leu Glu Leu Tyr Arg Tyr 230 235 240 AGT GGC GTA AAC ATG ACC GGG TTT GGG CTG CTT AAC ATT GAC AAC CCT 1281 Ser Gly Val Asn Met Thr Gly Phe Gly Leu Leu Asn Ile Asp Asn Pro 245 250 255 CAC GTG TCA TCC ATC ATT GAG AAG TGG TCC ATG GAG AGA CTG CAG GCC 1329 His Val Ser Ser Ile Ile Glu Lys Trp Ser Met Glu Arg Leu Gln Ala 260 265 270 CCA CCC AGG CCC GAG ACT GGC CTT TTG GAT GGC ATG ATG ACA ACT GAA 1377 Pro Pro Arg Pro Glu Thr Gly Leu Leu Asp Gly Met Met Thr Thr Glu 275 280 285 290 GCG GCT CTG ATG TAC GAT GCT GTG TAC ATG GTG GCC ATT GCC TCG CAC 1425 Ala Ala Leu Met Tyr Asp Ala Val Tyr Met Val Ala Ile Ala Ser His 295 300 305 CGG GCA TCC CAG CTG ACC GTC AGC TCC CTG CAG TGC CAT AGA CAT AAG 1473 Arg Ala Ser Gln Leu Thr Val Ser Ser Leu Gln Cys His Arg His Lys 310 315 320 CCA TGG CGC CTC GGA CCC AGA TTT ATG AAC CTG ATC AAA GAG GCC CGG 1521 Pro Trp Arg Leu Gly Pro Arg Phe Met Asn Leu Ile Lys Glu Ala Arg 325 330 335 TGG GAT GGC TTG ACT GGG CAT ATC ACC TTT AAT AAA ACC AAT GGC TTG 1569 Trp Asp Gly Leu Thr Gly His Ile Thr Phe Asn Lys Thr Asn Gly Leu 340 345 350 AGG AAG GAT TTT GAT CTG GAC ATT ATT AGT CTC AAA GAG GAA GGA ACT 1617 Arg Lys Asp Phe Asp Leu Asp Ile Ile Ser Leu Lys Glu Glu Gly Thr 355 360 365 370 GAA AAG ATT GGG ATT TGG AAT TCC AAC AGT GGG CTT AAC ATG ACG GAC 1665 Glu Lys Ile Gly Ile Trp Asn Ser Asn Ser Gly Leu Asn Met Thr Asp 375 380 385 AGC AAC AAA GAC AAG TCC AGC AAT ATC ACT GAT TCA TTG GCC AAC AGA 1713 Ser Asn Lys Asp Lys Ser Ser Asn Ile Thr Asp Ser Leu Ala Asn Arg 390 395 400 ACA CTC ATT GTC ACC ACC ATT CTG GAA GAA CCC TAT GTT ATG TAC AGG 1761 Thr Leu Ile Val Thr Thr Ile Leu Glu Glu Pro Tyr Val Met Tyr Arg 405 410 415 AAA TCT GAT AAG CCT CTA TAT GGA AAT GAC AGA TTT GAA GGA TAT TGC 1809 Lys Ser Asp Lys Pro Leu Tyr Gly Asn Asp Arg Phe Glu Gly Tyr Cys 420 425 430 CTA GAC CTG TTG AAA GAA TTG TCA AAC ATC CTG GGT TTC ATT TAT GAT 1857 Leu Asp Leu Leu Lys Glu Leu Ser Asn Ile Leu Gly Phe Ile Tyr Asp 435 440 445 450 GTT AAA CTA GTT CCC GAT GGC AAA TAT GGG GCC CAG AAT GAC AAA GGG 1905 Val Lys Leu Val Pro Asp Gly Lys Tyr Gly Ala Gln Asn Asp Lys Gly 455 460 465 GAG TGG AAC GGG ATG GTT AAA GAA CTC ATA GAT CAC AGG GCT GAC CTG 1953 Glu Trp Asn Gly Met Val Lys Glu Leu Ile Asp His Arg Ala Asp Leu 470 475 480 GCA GTG GCT CCT CTT ACC ATC ACC TAC GTG CGG GAG AAA GTC ATT GAC 2001 Ala Val Ala Pro Leu Thr Ile Thr Tyr Val Arg Glu Lys Val Ile Asp 485 490 495 TTC TCC AAA CCC TTC ATG ACC CTA GGC ATC AGC ATT CTC TAC CGG AAG 2049 Phe Ser Lys Pro Phe Met Thr Leu Gly Ile Ser Ile Leu Tyr Arg Lys 500 505 510 CCC AAT GGT ACC AAT CCA GGC GTT TTC TCC TTC CTC AAC CCC CTG TCT 2097 Pro Asn Gly Thr Asn Pro Gly Val Phe Ser Phe Leu Asn Pro Leu Ser 515 520 525 530 CCA GAT ATT TGG ATG TAT GTG CTC TTA GCC TGC TTG GGA GTC AGC TGT 2145 Pro Asp Ile Trp Met Tyr Val Leu Leu Ala Cys Leu Gly Val Ser Cys 535 540 545 GTA CTC TTT GTG ATT GCA AGG TTT ACA CCC TAC GAG TGG TAT AAC CCC 2193 Val Leu Phe Val Ile Ala Arg Phe Thr Pro Tyr Glu Trp Tyr Asn Pro 550 555 560 CAC CCA TGC AAC CCT GAC TCA GAC GTG GTG GAA AAC AAT TTT ACT TTA 2241 His Pro Cys Asn Pro Asp Ser Asp Val Val Glu Asn Asn Phe Thr Leu 565 570 575 CTA AAT AGT TTC TGG TTT GGA GTT GGA GCT CTC ATG CAG CAA GGA TCA 2289 Leu Asn Ser Phe Trp Phe Gly Val Gly Ala Leu Met Gln Gln Gly Ser 580 585 590 GAG CTG ATG CCC AAA GCT CTA TCG ACC AGA ATA GTT GGA GGG ATA TGG 2337 Glu Leu Met Pro Lys Ala Leu Ser Thr Arg Ile Val Gly Gly Ile Trp 595 600 605 610 TGG TTT TTC ACC CTA ATC ATC ATT TCA TCC TAC ACG GCC AAT CTG GCT 2385 Trp Phe Phe Thr Leu Ile Ile Ile Ser Ser Tyr Thr Ala Asn Leu Ala 615 620 625 GCC TTC TTG ACA GTA GAG AGA ATG GAA TCC CCC ATA GAT TCG GCA GAT 2433 Ala Phe Leu Thr Val Glu Arg Met Glu Ser Pro Ile Asp Ser Ala Asp 630 635 640 GAT CTG GCA AAG CAA ACC AAG ATA GAA TAT GGG GCG GTT AGA GAT GGA 2481 Asp Leu Ala Lys Gln Thr Lys Ile Glu Tyr Gly Ala Val Arg Asp Gly 645 650 655 TCA ACA ATG ACC TTC TTC AAG AAA TCA AAA ATC TCC ACC TAT GAG AAG 2529 Ser Thr Met Thr Phe Phe Lys Lys Ser Lys Ile Ser Thr Tyr Glu Lys 660 665 670 ATG TGG GCT TTC ATG AGC AGC AGG CAG CAG ACC GCC CTG GTA AGA AAC 2577 Met Trp Ala Phe Met Ser Ser Arg Gln Gln Thr Ala Leu Val Arg Asn 675 680 685 690 AGT GAT GAG GGG ATC CAG AGA GTG CTC ACC ACA GAC TAC GCG CTG CTG 2625 Ser Asp Glu Gly Ile Gln Arg Val Leu Thr Thr Asp Tyr Ala Leu Leu 695 700 705 ATG GAG TCC ACC AGC ATT GAG TAT GTG ACG CAG AGA AAC TGC AAC CTC 2673 Met Glu Ser Thr Ser Ile Glu Tyr Val Thr Gln Arg Asn Cys Asn Leu 710 715 720 ACT CAG ATC GGG GGC CTC ATT GAC TCC AAA GGT TAC GGA GTG GGA ACA 2721 Thr Gln Ile Gly Gly Leu Ile Asp Ser Lys Gly Tyr Gly Val Gly Thr 725 730 735 CCT ATT GGT TCT CCT TAC CGG GAT AAA ATT ACT ATT GCT ATT CTT CAA 2769 Pro Ile Gly Ser Pro Tyr Arg Asp Lys Ile Thr Ile Ala Ile Leu Gln 740 745 750 CTC CAA GAA GAA GGG AAG CTG CAT ATG ATG AAA GAG AAG TGG TGG CGT 2817 Leu Gln Glu Glu Gly Lys Leu His Met Met Lys Glu Lys Trp Trp Arg 755 760 765 770 GGG AAT GGC TGC CCC GAG GAA GAC AAC AAA GAA GCC AGT GCC CTG GGA 2865 Gly Asn Gly Cys Pro Glu Glu Asp Asn Lys Glu Ala Ser Ala Leu Gly 775 780 785 GTG GAA AAT ATT GGA GGC ATC TTC ATT GTT CTG GCT GCC GGA CTG GTC 2913 Val Glu Asn Ile Gly Gly Ile Phe Ile Val Leu Ala Ala Gly Leu Val 790 795 800 CTT TCT GTA TTT GTA GCT ATT GGA GAA TTC ATA TAC AAA TCA CGG AAG 2961 Leu Ser Val Phe Val Ala Ile Gly Glu Phe Ile Tyr Lys Ser Arg Lys 805 810 815 AAT AAT GAT ATT GAA CAG TGT CTC TCT TTC AAC GCT ATC ATG GAA GAA 3009 Asn Asn Asp Ile Glu Gln Cys Leu Ser Phe Asn Ala Ile Met Glu Glu 820 825 830 CTG GGA ATC TCA CTG AAG AAT CAG AAA AAA ATA AAG AAA AAG TCA AGA 3057 Leu Gly Ile Ser Leu Lys Asn Gln Lys Lys Ile Lys Lys Lys Ser Arg 835 840 845 850 ACT AAG GGG AAA TCT TCC TTC ACA AGT ATC CTT ACT TGT CAT CAG AGA 3105 Thr Lys Gly Lys Ser Ser Phe Thr Ser Ile Leu Thr Cys His Gln Arg 855 860 865 CGA ACT CAG AGA AAA GAG ACT GTG GCG TGATCCAAGG AAACGCCTGT 3152 Arg Thr Gln Arg Lys Glu Thr Val Ala 870 875 AGGAAGAAAA AGGATGCATT CCCTACAGAT TTTTGGAGAA AGGATTTCTG AGGAGTTGTG 3212 TGATGTGTTT CCATATATCT ATATCCATAA CTCTGATTAT GAATACAGAT ATAAGAAATA 3272 CAAAAGTTTA AAAAGCTCAC ATAGATATGA CTTGGGAAGT GACACCAGTT CTTTTAAAAT 3332 AAATTTGTAT GCACAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAGGAA TTC 3385 905 amino acids amino acid linear protein 2 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp -30 -25 -20 -15 Thr Ser Trp Ala Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr -10 -5 1 Ala Pro Gln Val Leu Arg Ile Gly Gly Ile Phe Glu Thr Val Glu Asn 5 10 15 Glu Pro Val Asn Val Glu Glu Leu Ala Phe Lys Phe Ala Val Thr Ser 20 25 30 Ile Asn Arg Asn Arg Thr Leu Met Pro Asn Thr Thr Leu Thr Tyr Asp 35 40 45 50 Ile Gln Arg Ile Asn Leu Phe Asp Ser Phe Glu Ala Ser Arg Arg Ala 55 60 65 Cys Asp Gln Leu Ala Leu Gly Val Ala Ala Leu Phe Gly Pro Ser His 70 75 80 Ser Ser Ser Val Ser Ala Val Gln Ser Ile Cys Asn Ala Leu Glu Val 85 90 95 Pro His Ile Gln Thr Arg Trp Lys His Pro Ser Val Asp Asn Lys Asp 100 105 110 Leu Phe Tyr Ile Asn Leu Tyr Pro Asp Tyr Ala Ala Ile Ser Arg Ala 115 120 125 130 Ile Leu Asp Leu Val Leu Tyr Tyr Asn Trp Lys Thr Val Thr Val Val 135 140 145 Tyr Glu Asp Ser Thr Gly Leu Ile Arg Leu Gln Glu Leu Ile Lys Ala 150 155 160 Pro Ser Arg Tyr Asn Ile Lys Ile Lys Ile Arg Gln Leu Pro Ser Gly 165 170 175 Asn Lys Asp Ala Lys Pro Leu Leu Lys Glu Met Lys Lys Gly Lys Glu 180 185 190 Phe Tyr Val Ile Phe Asp Cys Ser His Glu Thr Ala Ala Glu Ile Leu 195 200 205 210 Lys Gln Ile Leu Phe Met Gly Met Met Thr Glu Tyr Tyr His Tyr Phe 215 220 225 Phe Thr Thr Leu Asp Leu Phe Ala Leu Asp Leu Glu Leu Tyr Arg Tyr 230 235 240 Ser Gly Val Asn Met Thr Gly Phe Gly Leu Leu Asn Ile Asp Asn Pro 245 250 255 His Val Ser Ser Ile Ile Glu Lys Trp Ser Met Glu Arg Leu Gln Ala 260 265 270 Pro Pro Arg Pro Glu Thr Gly Leu Leu Asp Gly Met Met Thr Thr Glu 275 280 285 290 Ala Ala Leu Met Tyr Asp Ala Val Tyr Met Val Ala Ile Ala Ser His 295 300 305 Arg Ala Ser Gln Leu Thr Val Ser Ser Leu Gln Cys His Arg His Lys 310 315 320 Pro Trp Arg Leu Gly Pro Arg Phe Met Asn Leu Ile Lys Glu Ala Arg 325 330 335 Trp Asp Gly Leu Thr Gly His Ile Thr Phe Asn Lys Thr Asn Gly Leu 340 345 350 Arg Lys Asp Phe Asp Leu Asp Ile Ile Ser Leu Lys Glu Glu Gly Thr 355 360 365 370 Glu Lys Ile Gly Ile Trp Asn Ser Asn Ser Gly Leu Asn Met Thr Asp 375 380 385 Ser Asn Lys Asp Lys Ser Ser Asn Ile Thr Asp Ser Leu Ala Asn Arg 390 395 400 Thr Leu Ile Val Thr Thr Ile Leu Glu Glu Pro Tyr Val Met Tyr Arg 405 410 415 Lys Ser Asp Lys Pro Leu Tyr Gly Asn Asp Arg Phe Glu Gly Tyr Cys 420 425 430 Leu Asp Leu Leu Lys Glu Leu Ser Asn Ile Leu Gly Phe Ile Tyr Asp 435 440 445 450 Val Lys Leu Val Pro Asp Gly Lys Tyr Gly Ala Gln Asn Asp Lys Gly 455 460 465 Glu Trp Asn Gly Met Val Lys Glu Leu Ile Asp His Arg Ala Asp Leu 470 475 480 Ala Val Ala Pro Leu Thr Ile Thr Tyr Val Arg Glu Lys Val Ile Asp 485 490 495 Phe Ser Lys Pro Phe Met Thr Leu Gly Ile Ser Ile Leu Tyr Arg Lys 500 505 510 Pro Asn Gly Thr Asn Pro Gly Val Phe Ser Phe Leu Asn Pro Leu Ser 515 520 525 530 Pro Asp Ile Trp Met Tyr Val Leu Leu Ala Cys Leu Gly Val Ser Cys 535 540 545 Val Leu Phe Val Ile Ala Arg Phe Thr Pro Tyr Glu Trp Tyr Asn Pro 550 555 560 His Pro Cys Asn Pro Asp Ser Asp Val Val Glu Asn Asn Phe Thr Leu 565 570 575 Leu Asn Ser Phe Trp Phe Gly Val Gly Ala Leu Met Gln Gln Gly Ser 580 585 590 Glu Leu Met Pro Lys Ala Leu Ser Thr Arg Ile Val Gly Gly Ile Trp 595 600 605 610 Trp Phe Phe Thr Leu Ile Ile Ile Ser Ser Tyr Thr Ala Asn Leu Ala 615 620 625 Ala Phe Leu Thr Val Glu Arg Met Glu Ser Pro Ile Asp Ser Ala Asp 630 635 640 Asp Leu Ala Lys Gln Thr Lys Ile Glu Tyr Gly Ala Val Arg Asp Gly 645 650 655 Ser Thr Met Thr Phe Phe Lys Lys Ser Lys Ile Ser Thr Tyr Glu Lys 660 665 670 Met Trp Ala Phe Met Ser Ser Arg Gln Gln Thr Ala Leu Val Arg Asn 675 680 685 690 Ser Asp Glu Gly Ile Gln Arg Val Leu Thr Thr Asp Tyr Ala Leu Leu 695 700 705 Met Glu Ser Thr Ser Ile Glu Tyr Val Thr Gln Arg Asn Cys Asn Leu 710 715 720 Thr Gln Ile Gly Gly Leu Ile Asp Ser Lys Gly Tyr Gly Val Gly Thr 725 730 735 Pro Ile Gly Ser Pro Tyr Arg Asp Lys Ile Thr Ile Ala Ile Leu Gln 740 745 750 Leu Gln Glu Glu Gly Lys Leu His Met Met Lys Glu Lys Trp Trp Arg 755 760 765 770 Gly Asn Gly Cys Pro Glu Glu Asp Asn Lys Glu Ala Ser Ala Leu Gly 775 780 785 Val Glu Asn Ile Gly Gly Ile Phe Ile Val Leu Ala Ala Gly Leu Val 790 795 800 Leu Ser Val Phe Val Ala Ile Gly Glu Phe Ile Tyr Lys Ser Arg Lys 805 810 815 Asn Asn Asp Ile Glu Gln Cys Leu Ser Phe Asn Ala Ile Met Glu Glu 820 825 830 Leu Gly Ile Ser Leu Lys Asn Gln Lys Lys Ile Lys Lys Lys Ser Arg 835 840 845 850 Thr Lys Gly Lys Ser Ser Phe Thr Ser Ile Leu Thr Cys His Gln Arg 855 860 865 Arg Thr Gln Arg Lys Glu Thr Val Ala 870 875 50 amino acids amino acid linear peptide internal 3 Ala Ala Phe Leu Thr Val Glu Arg Met Glu Ser Pro Ile Asn Ser Ala 1 5 10 15 Asp Asp Leu Ala Lys Gln Thr Lys Ile Glu Tyr Gly Ala Val Arg Asp 20 25 30 Gly Ser Thr Met Thr Phe Phe Lys Lys Ser Lys Ile Ser Thr Tyr Glu 35 40 45 Lys Met 50 50 amino acids amino acid linear peptide internal 4 Ala Ala Phe Leu Thr Val Glu Arg Met Glu Ser Pro Ile Asp Ser Ala 1 5 10 15 Asp Asp Leu Ala Lys Gln Thr Lys Ile Glu Tyr Gly Ala Val Arg Asp 20 25 30 Gly Ser Thr Met Thr Phe Phe Lys Lys Ser Lys Ile Ser Thr Tyr Glu 35 40 45 Lys Met 50 50 base pairs nucleic acid double linear cDNA 5 GAGAGAATGG AATCCCCCAT AAATTCGGCA GATGATCTGG CAAAGCAAAC 50 50 base pairs nucleic acid double linear cDNA 6 GAGAGAATGG AATCCCCCAT AGATTCGGCA GATGATCTGG CAAAGCAAAC 50 38 amino acids amino acid linear peptide C-terminal 7 Ala Ala Gly Leu Val Leu Ser Val Phe Val Ala Ile Gly Glu Phe Ile 1 5 10 15 Tyr Lys Ser Arg Lys Asn Asn Asp Ile Glu Gln Val Ser His Leu Phe 20 25 30 Leu Gly Leu Val Ser Leu 35 50 amino acids amino acid linear peptide internal 8 Ala Ala Gly Leu Val Leu Ser Val Phe Val Ala Ile Gly Glu Phe Ile 1 5 10 15 Tyr Lys Ser Arg Lys Asn Asn Asp Ile Glu Gln Cys Leu Ser Phe Asp 20 25 30 Ala Ile Met Glu Glu Leu Gly Ile Ser Leu Lys Asn Gln Lys Lys Ile 35 40 45 Lys Lys 50 119 base pairs nucleic acid double linear cDNA 9 CAAATCACGG AAGAATAATG ATATTGAACA GGTGAGTCAT CTCTTTCTAG GACTGGTTAG 60 TTTATAGTTT GCATTATCTG TCTTAAGTTT GGGGGTTTTT AAGGATGTTT GCTCTTTTT 119 124 base pairs nucleic acid double linear cDNA 10 CAAATCACGG AAGAATAATG ATATTGAACA GTGTCTCTCT TTCAACGCTA TCATGGAAGA 60 ACTGGGAATC TCACTGAAGA ATCAGAAAAA AATAAAGAAA AAGTCAAGAA CTAAGGGGAA 120 ATCT 124 44 amino acids amino acid linear peptide N-terminal Peptide 1..29 /note= “Signal Peptide” 11 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp 1 5 10 15 Thr Ser Trp Gly Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr 20 25 30 Ala Pro Gln Val Leu Arg Ile Ala Cys Asp Gln Leu 35 40 100 amino acids amino acid linear peptide N-terminal Peptide 1..29 /note= “Signal Peptide” 12 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp 1 5 10 15 Thr Ser Trp Gly Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr 20 25 30 Ala Pro Gln Val Leu Arg Ile Gly Gly Ile Phe Glu Thr Val Glu Asn 35 40 45 Glu Pro Val Asn Val Glu Glu Leu Ala Phe Lys Phe Ala Val Thr Ser 50 55 60 Ile Asn Arg Asn Arg Thr Leu Met Pro Asn Thr Thr Leu Thr Tyr Asp 65 70 75 80 Ile Gln Arg Ile Asn Leu Phe Asp Ser Phe Glu Val Leu Arg Ile Ala 85 90 95 Cys Asp Gln Leu 100 82 base pairs nucleic acid double linear cDNA 13 ATCCTCCCTC AGACCGCCCC GCAAGTACTC AGGATCGCAT GTGACCAGCT GGCTCTTGGT 60 GTGGCTGCTC TCTTTGGCCC TT 82 100 base pairs nucleic acid double linear cDNA 14 ATCCTCCCTC AGACCGCCCC GCAAGTACTC AGGATCGGAG GGATTTTTGA GAGAGCATGT 60 GACCAGCTGG CTCTTGGTGT GGCTGCTCTC TTTGGCCCTT 100 40 base pairs nucleic acid single linear 15 ATCGGCGGCA TCTTCATTGT TCTGGCTGCA GGACTCGTGC 40 20 base pairs nucleic acid single linear 16 CCATCATTGA GAAGTGGTCC 20 13 base pairs nucleic acid double linear cDNA 17 AGCTTGCCGC CGC 13 893 amino acids amino acid <Unknown> linear protein 18 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp 1 5 10 15 Thr Ser Trp Ala Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr 20 25 30 Ala Pro Gln Val Leu Arg Ile Gly Gly Ile Phe Glu Thr Val Glu Asn 35 40 45 Glu Pro Val Asn Val Glu Glu Leu Ala Phe Lys Phe Ala Val Thr Ser 50 55 60 Ile Asn Arg Asn Arg Thr Leu Met Pro Asn Thr Thr Leu Thr Tyr Asp 65 70 75 80 Ile Gln Arg Ile Asn Leu Phe Asp Ser Phe Glu Ala Ser Arg Arg Ala 85 90 95 Cys Asp Gln Leu Ala Leu Gly Val Ala Ala Leu Phe Gly Pro Ser His 100 105 110 Ser Ser Ser Val Ser Ala Val Gln Ser Ile Cys Asn Ala Leu Glu Val 115 120 125 Pro His Ile Gln Thr Arg Trp Lys His Pro Ser Val Asp Asn Lys Asp 130 135 140 Leu Phe Tyr Ile Asn Leu Tyr Pro Asp Tyr Ala Ala Ile Ser Arg Ala 145 150 155 160 Ile Leu Asp Leu Val Leu Tyr Tyr Asn Trp Lys Thr Val Thr Val Val 165 170 175 Tyr Glu Asp Ser Thr Gly Leu Ile Arg Leu Gln Glu Leu Ile Lys Ala 180 185 190 Pro Ser Arg Tyr Asn Ile Lys Ile Lys Ile Arg Gln Leu Pro Ser Gly 195 200 205 Asn Lys Asp Ala Lys Pro Leu Leu Lys Glu Met Lys Lys Gly Lys Glu 210 215 220 Phe Tyr Val Ile Phe Asp Cys Ser His Glu Thr Ala Ala Glu Ile Leu 225 230 235 240 Lys Gln Ile Leu Phe Met Gly Met Met Thr Glu Tyr Tyr His Tyr Phe 245 250 255 Phe Thr Thr Leu Asp Leu Phe Ala Leu Asp Leu Glu Leu Tyr Arg Tyr 260 265 270 Ser Gly Val Asn Met Thr Gly Phe Gly Leu Leu Asn Ile Asp Asn Pro 275 280 285 His Val Ser Ser Ile Ile Glu Lys Trp Ser Met Glu Arg Leu Gln Ala 290 295 300 Pro Pro Arg Pro Glu Thr Gly Leu Leu Asp Gly Met Met Thr Thr Glu 305 310 315 320 Ala Ala Leu Met Tyr Asp Ala Val Tyr Met Val Ala Ile Ala Ser His 325 330 335 Arg Ala Ser Gln Leu Thr Val Ser Ser Leu Gln Cys His Arg His Lys 340 345 350 Pro Trp Arg Leu Gly Pro Arg Phe Met Asn Leu Ile Lys Glu Ala Arg 355 360 365 Trp Asp Gly Leu Thr Gly His Ile Thr Phe Asn Lys Thr Asn Gly Leu 370 375 380 Arg Lys Asp Phe Asp Leu Asp Ile Ile Ser Leu Lys Glu Glu Gly Thr 385 390 395 400 Glu Lys Ile Gly Ile Trp Asn Ser Asn Ser Gly Leu Asn Met Thr Asp 405 410 415 Ser Asn Lys Asp Lys Ser Ser Asn Ile Thr Asp Ser Leu Ala Asn Arg 420 425 430 Thr Leu Ile Val Thr Thr Ile Leu Glu Glu Pro Tyr Val Met Tyr Arg 435 440 445 Lys Ser Asp Lys Pro Leu Tyr Gly Asn Asp Arg Phe Glu Gly Tyr Cys 450 455 460 Leu Asp Leu Leu Lys Glu Leu Ser Asn Ile Leu Gly Phe Ile Tyr Asp 465 470 475 480 Val Lys Leu Val Pro Asp Gly Lys Tyr Gly Ala Gln Asn Asp Lys Gly 485 490 495 Glu Trp Asn Gly Met Val Lys Glu Leu Ile Asp His Arg Ala Asp Leu 500 505 510 Ala Val Ala Pro Leu Thr Ile Thr Tyr Val Arg Glu Lys Val Ile Asp 515 520 525 Phe Ser Lys Pro Phe Met Thr Leu Gly Ile Ser Ile Leu Tyr Arg Lys 530 535 540 Pro Asn Gly Thr Asn Pro Gly Val Phe Ser Phe Leu Asn Pro Leu Ser 545 550 555 560 Pro Asp Ile Trp Met Tyr Val Leu Leu Ala Cys Leu Gly Val Ser Cys 565 570 575 Val Leu Phe Val Ile Ala Arg Phe Thr Pro Tyr Glu Trp Tyr Asn Pro 580 585 590 His Pro Cys Asn Pro Asp Ser Asp Val Val Glu Asn Asn Phe Thr Leu 595 600 605 Leu Asn Ser Phe Trp Phe Gly Val Gly Ala Leu Met Gln Gln Gly Ser 610 615 620 Glu Leu Met Pro Lys Ala Leu Ser Thr Arg Ile Val Gly Gly Ile Trp 625 630 635 640 Trp Phe Phe Thr Leu Ile Ile Ile Ser Ser Tyr Thr Ala Asn Leu Ala 645 650 655 Ala Phe Leu Thr Val Glu Arg Met Glu Ser Pro Ile Asp Ser Ala Asp 660 665 670 Asp Leu Ala Lys Gln Thr Lys Ile Glu Tyr Gly Ala Val Arg Asp Gly 675 680 685 Ser Thr Met Thr Phe Phe Lys Lys Ser Lys Ile Ser Thr Tyr Glu Lys 690 695 700 Met Trp Ala Phe Met Ser Ser Arg Gln Gln Thr Ala Leu Val Arg Asn 705 710 715 720 Ser Asp Glu Gly Ile Gln Arg Val Leu Thr Thr Asp Tyr Ala Leu Leu 725 730 735 Met Glu Ser Thr Ser Ile Glu Tyr Val Thr Gln Arg Asn Cys Asn Leu 740 745 750 Thr Gln Ile Gly Gly Leu Ile Asp Ser Lys Gly Tyr Gly Val Gly Thr 755 760 765 Pro Ile Gly Ser Pro Tyr Arg Asp Lys Ile Thr Ile Ala Ile Leu Gln 770 775 780 Leu Gln Glu Glu Gly Lys Leu His Met Met Lys Glu Lys Trp Trp Arg 785 790 795 800 Gly Asn Gly Cys Pro Glu Glu Asp Asn Lys Glu Ala Ser Ala Leu Gly 805 810 815 Val Glu Asn Ile Gly Gly Ile Phe Ile Val Leu Ala Ala Gly Leu Val 820 825 830 Leu Ser Val Phe Val Ala Ile Gly Glu Phe Ile Tyr Lys Ser Arg Lys 835 840 845 Asn Asn Asp Ile Glu Gln Val Ser His Leu Phe Leu Gly Leu Val Ser 850 855 860 Leu Lys Ser Arg Thr Lys Gly Lys Ser Ser Phe Thr Ser Ile Leu Thr 865 870 875 880 Cys His Gln Arg Arg Thr Gln Arg Lys Glu Thr Val Ala 885 890 849 amino acids amino acid <Unknown> linear protein 19 Met Glu His Gly Thr Leu Leu Ala Gln Pro Gly Leu Trp Thr Arg Asp 1 5 10 15 Thr Ser Trp Ala Leu Leu Tyr Phe Leu Cys Tyr Ile Leu Pro Gln Thr 20 25 30 Ala Pro Gln Ala Ser Arg Arg Ala Cys Asp Gln Leu Ala Leu Gly Val 35 40 45 Ala Ala Leu Phe Gly Pro Ser His Ser Ser Ser Val Ser Ala Val Gln 50 55 60 Ser Ile Cys Asn Ala Leu Glu Val Pro His Ile Gln Thr Arg Trp Lys 65 70 75 80 His Pro Ser Val Asp Asn Lys Asp Leu Phe Tyr Ile Asn Leu Tyr Pro 85 90 95 Asp Tyr Ala Ala Ile Ser Arg Ala Ile Leu Asp Leu Val Leu Tyr Tyr 100 105 110 Asn Trp Lys Thr Val Thr Val Val Tyr Glu Asp Ser Thr Gly Leu Ile 115 120 125 Arg Leu Gln Glu Leu Ile Lys Ala Pro Ser Arg Tyr Asn Ile Lys Ile 130 135 140 Lys Ile Arg Gln Leu Pro Ser Gly Asn Lys Asp Ala Lys Pro Leu Leu 145 150 155 160 Lys Glu Met Lys Lys Gly Lys Glu Phe Tyr Val Ile Phe Asp Cys Ser 165 170 175 His Glu Thr Ala Ala Glu Ile Leu Lys Gln Ile Leu Phe Met Gly Met 180 185 190 Met Thr Glu Tyr Tyr His Tyr Phe Phe Thr Thr Leu Asp Leu Phe Ala 195 200 205 Leu Asp Leu Glu Leu Tyr Arg Tyr Ser Gly Val Asn Met Thr Gly Phe 210 215 220 Gly Leu Leu Asn Ile Asp Asn Pro His Val Ser Ser Ile Ile Glu Lys 225 230 235 240 Trp Ser Met Glu Arg Leu Gln Ala Pro Pro Arg Pro Glu Thr Gly Leu 245 250 255 Leu Asp Gly Met Met Thr Thr Glu Ala Ala Leu Met Tyr Asp Ala Val 260 265 270 Tyr Met Val Ala Ile Ala Ser His Arg Ala Ser Gln Leu Thr Val See 275 280 285 Ser Leu Gln Cys His Arg His Lys Pro Trp Arg Leu Gly Pro Arg Phe 290 295 300 Met Asn Leu Ile Lys Glu Ala Arg Trp Asp Gly Leu Thr Gly His Ile 305 310 315 320 Thr Phe Asn Lys Thr Asn Gly Leu Arg Lys Asp Phe Asp Leu Asp Ile 325 330 335 Ile Ser Leu Lys Glu Glu Gly Thr Glu Lys Ile Gly Ile Trp Asn Ser 340 345 350 Asn Ser Gly Leu Asn Met Thr Asp Ser Asn Lys Asp Lys Ser Ser Asn 355 360 365 Ile Thr Asp Ser Leu Ala Asn Arg Thr Leu Ile Val Thr Thr Ile Leu 370 375 380 Glu Glu Pro Tyr Val Met Tyr Arg Lys Ser Asp Lys Pro Leu Tyr Gly 385 390 395 400 Asn Asp Arg Phe Glu Gly Tyr Cys Leu Asp Leu Leu Lys Glu Leu Ser 405 410 415 Asn Ile Leu Gly Phe Ile Tyr Asp Val Lys Leu Val Pro Asp Gly Lys 420 425 430 Tyr Gly Ala Gln Asn Asp Lys Gly Glu Trp Asn Gly Met Val Lys Glu 435 440 445 Leu Ile Asp His Arg Ala Asp Leu Ala Val Ala Pro Leu Thr Ile Thr 450 455 460 Tyr Val Arg Glu Lys Val Ile Asp Phe Ser Lys Pro Phe Met Thr Leu 465 470 475 480 Gly Ile Ser Ile Leu Tyr Arg Lys Pro Asn Gly Thr Asn Pro Gly Val 485 490 495 Phe Ser Phe Leu Asn Pro Leu Ser Pro Asp Ile Trp Met Tyr Val Leu 500 505 510 Leu Ala Cys Leu Gly Val Ser Cys Val Leu Phe Val Ile Ala Arg Phe 515 520 525 Thr Pro Tyr Glu Trp Tyr Asn Pro His Pro Cys Asn Pro Asp Ser Asp 530 535 540 Val Val Glu Asn Asn Phe Thr Leu Leu Asn Ser Phe Trp Phe Gly Val 545 550 555 560 Gly Ala Leu Met Gln Gln Gly Ser Glu Leu Met Pro Lys Ala Leu Ser 565 570 575 Thr Arg Ile Val Gly Gly Ile Trp Trp Phe Phe Thr Leu Ile Ile Ile 580 585 590 Ser Ser Tyr Thr Ala Asn Leu Ala Ala Phe Leu Thr Val Glu Arg Met 595 600 605 Glu Ser Pro Ile Asp Ser Ala Asp Asp Leu Ala Lys Gln Thr Lys Ile 610 615 620 Glu Tyr Gly Ala Val Arg Asp Gly Ser Thr Met Thr Phe Phe Lys Lys 625 630 635 640 Ser Lys Ile Ser Thr Tyr Glu Lys Met Trp Ala Phe Met Ser Ser Arg 645 650 655 Gln Gln Thr Ala Leu Val Arg Asn Ser Asp Glu Gly Ile Gln Arg Val 660 665 670 Leu Thr Thr Asp Tyr Ala Leu Leu Met Glu Ser Thr Ser Ile Glu Tyr 675 680 685 Val Thr Gln Arg Asn Cys Asn Leu Thr Gln Ile Gly Gly Leu Ile Asp 690 695 700 Ser Lys Gly Tyr Gly Val Gly Thr Pro Ile Gly Ser Pro Tyr Arg Asp 705 710 715 720 Lys Ile Thr Ile Ala Ile Leu Gln Leu Gln Glu Glu Gly Lys Leu His 725 730 735 Met Met Lys Glu Lys Trp Trp Arg Gly Asn Gly Cys Pro Glu Glu Asp 740 745 750 Asn Lys Glu Ala Ser Ala Leu Gly Val Glu Asn Ile Gly Gly Ile Phe 755 760 765 Ile Val Leu Ala Ala Gly Leu Val Leu Ser Val Phe Val Ala Ile Gly 770 775 780 Glu Phe Ile Tyr Lys Ser Arg Lys Asn Asn Asp Ile Glu Gln Cys Leu 785 790 795 800 Ser Phe Asn Ala Ile Met Glu Glu Leu Gly Ile Ser Leu Lys Asn Gln 805 810 815 Lys Lys Ile Lys Lys Lys Ser Arg Thr Lys Gly Lys Ser Ser Phe Thr 820 825 830 Ser Ile Leu Thr Cys His Gln Arg Arg Thr Gln Arg Lys Glu Thr Val 835 840 845 Ala 

We claim:
 1. A method of assaying a test ligand for binding to a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA receptor, and then determining the extent of binding between the human EAA receptor and the test ligand, wherein said cell has been engineered genetically to produce a kainate-binding human EAA receptor having incorporated expressibly therein a heterologous DNA molecule that codes for a human EAA3 receptor selected from the group consisting of: (a) a human EAA3a receptor having the amino acid sequence of SEQ ID NO:2; (b) a human EAA3b receptor having the amino acid sequence of SEQ ID NO:2 with the exception that the amino acid at position 639 is asparagine instead of aspartate; (c) a human EAA3c receptor having the amino acid sequence of SEQ ID NO:18, and (d) a human EAA3d receptor having the amino acid sequence of SEQ ID NO:19.
 2. A method according to claim 1, wherein the cell is a mammalian cell.
 3. A method according to claim 1, wherein the test ligand is incubated with a membrane preparation derived from said human EAA3-producing cell.
 4. A method according to claim 1, wherein said DNA codes for the human EAA3a receptor.
 5. A method according to claim 1, wherein said DNA codes for the human EAA3b receptor.
 6. A method of assaying a test ligand for binding to a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA3c receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA3c receptor, and then determining the extent of binding between the human EAA3c receptor and the test ligand, wherein said cell has been engineered genetically to produce a kainate-binding human EAA3c receptor having the amino acid sequence of SEQ ID NO:18.
 7. A method of assaying a test ligand for binding to a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA3d receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA3d receptor, and then determining the extent of binding between the human EAA3d receptor and the test ligand, wherein said cell has been engineered genetically to produce a kainate-binding human EAA3d receptor having the amino acid sequence of SEQ ID NO:19.
 8. A method of assaying a test ligand for interaction with a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA3 receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA3 receptor, and then determining the ligand-induced electrical current across said cell or membrane, wherein said cell has been engineered genetically to produce a kainate-binding human EAA receptor having incorporated expressibly therein a heterologous DNA molecule that codes for a human EAA3 receptor selected from the group consisting of: (a) a human EAA3a receptor having the amino acid sequence of SEQ ID NO:2; (b) a human EAA3b receptor having the amino acid sequence of SEQ ID NO:2 with the exception that the amino acid at position 639 is asparagine instead of aspartate; (c) a human EAA3c receptor having the amino acid sequence of SEQ ID NO:18, and (d) a human EAA3d receptor having the amino acid sequence of SEQ ID NO:19.
 9. A method according to claim 8, wherein said DNA codes for the human EAA3a receptor.
 10. A method according to claim 8, wherein said DNA codes for the human EAA3b receptor.
 11. A method of assaying a test ligand for interaction with a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA3c receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA3c receptor, and then determining the ligand-induced electrical current across said cell or membrane, wherein said cell has been engineered genetically to produce a kainate-binding human EAA3c receptor having incorporated expressibly therein a heterologous DNA molecule that codes for a human EAA3c receptor having the amino acid sequence of SEQ ID NO:18.
 12. A method of assaying a test ligand for interaction with a human CNS receptor, which comprises the steps of incubating the test ligand under appropriate conditions with a human EAA3d receptor-producing cell, or with a membrane preparation derived therefrom which contains said EAA3d receptor and then determining the ligand-induced electrical current across said cell or membrane, wherein said cell has been engineered genetically to produce a kainate-binding human EAA3d receptor having incorporated expressibly therein a heterologous DNA molecule that codes for a human EAA3d receptor having the amino acid sequence of SEQ ID NO:19. 